CEMAX SCANLINK V— 510(k) K943357

Substantially Equivalent

Cemax, Inc.

FDA 510(k) clearance K943357 for CEMAX SCANLINK V, Substantially Equivalent on 1994-11-22. Applicant: Cemax, Inc..

Clearance details

Applicant: Cemax, Inc.
Product code: Code LMA
Advisory panel: Radiology
Date received: 1994-07-12
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fremont, CA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.